rel-tert-Butyl (3bS,6aS)-3-iodo-1,3b,4,6,6a,7-hexahydro-5H-pyrrolo[3',4':3,4]cyclopenta[1,2-c]pyrazole-5-carboxylate
95%
- Product Code: 87745
CAS:
1251016-05-3
| Molecular Weight: | 375.21 g./mol | Molecular Formula: | C₁₃H₁₈IN₃O₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD17016566 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, sealed, dry |
Product Description:
This compound is primarily utilized in organic synthesis as a key intermediate for the development of complex molecular structures, particularly in pharmaceutical research. Its unique structure, featuring an iodine atom and a pyrrolo-pyrazole core, makes it valuable for constructing biologically active molecules. It is often employed in medicinal chemistry for designing potential drug candidates, especially in the exploration of enzyme inhibitors or receptor modulators. The iodine moiety allows for further functionalization through cross-coupling reactions, enabling the synthesis of diverse derivatives. Additionally, its stereochemistry is critical for creating enantiomerically pure compounds, which are essential in drug development to ensure specificity and efficacy.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | $1,232.13 |
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rel-tert-Butyl (3bS,6aS)-3-iodo-1,3b,4,6,6a,7-hexahydro-5H-pyrrolo[3',4':3,4]cyclopenta[1,2-c]pyrazole-5-carboxylate
This compound is primarily utilized in organic synthesis as a key intermediate for the development of complex molecular structures, particularly in pharmaceutical research. Its unique structure, featuring an iodine atom and a pyrrolo-pyrazole core, makes it valuable for constructing biologically active molecules. It is often employed in medicinal chemistry for designing potential drug candidates, especially in the exploration of enzyme inhibitors or receptor modulators. The iodine moiety allows for further functionalization through cross-coupling reactions, enabling the synthesis of diverse derivatives. Additionally, its stereochemistry is critical for creating enantiomerically pure compounds, which are essential in drug development to ensure specificity and efficacy.
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